Impact of a psycho-education program for victims of sexual violence
Evaluation of the Impact of Participation in a Psycho-education Program for Victims of Sexual Violence
This study tests a group program for victims of sexual violence to see if it helps improve their mental health and reduce PTSD symptoms.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Sponsor | Centre Hospitalier Charles Perrens, Bordeaux Government |
| Locations | 1 site (Bordeaux) |
| Trial ID | NCT06718387 on ClinicalTrials.gov |
What this trial studies
This study evaluates a psycho-education program designed for victims of sexual violence to determine its effectiveness in improving patient outcomes. The program involves group sessions facilitated by trained therapists and includes the participation of a patient-partner who contributes to the design and facilitation of the sessions. The study aims to assess the impact of this intervention on patients' mental health, specifically focusing on PTSD symptoms. Participants are selected based on recommendations from therapists at the Centre Hospitalier Charles Perrens.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals who have been treated at the Centre Hospitalier and have experienced sexual violence.
Not a fit: Patients who have not been exposed to sexual violence or are not receiving treatment at the Centre Hospitalier may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve the mental health and therapeutic alliance of victims of sexual violence.
How similar studies have performed: Other studies have shown positive outcomes with psycho-education programs for trauma victims, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * At the suggestion of CRP therapists, * Patient treated at the CRP having been exposed to sexual violence Exclusion Criteria: \-
Where this trial is running
Bordeaux
- Centre Hospitalier Charles PERRENS — Bordeaux, France (Recruiting)
Study contacts
- Principal investigator: Chantal BERGEY — Charles Perrens
- Study coordinator: Chantal BERGEY, MD
- Email: cbergey@ch-perrens.fr
- Phone: 05 56 56 35 78
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.